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Structure of 748812-37-5
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5-Bromo-3-fluoropyridin-2-amine features a strategically positioned bromine and fluorine substituent on a pyridine scaffold, enabling selective functionalization in cross-coupling reactions. The electron-deficient ring system enhances reactivity in palladium-catalyzed transformations, while the amine group serves as a direct handle for derivatization. This bench-stable intermediate is well-suited for medicinal chemistry and materials synthesis workflows.
5-Bromo-3-fluoropyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogen reactivity. The bromine and fluorine substituents offer orthogonal functionalization potential, while the pyridin-2-amine moiety provides a robust nitrogen handle for derivatization. This compound exhibits excellent bench stability and facilitates efficient synthesis of complex heterocyclic scaffolds relevant to pharmaceutical development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H312-H315-H319-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P341-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: